跳转至内容
Merck
CN

B4856

Sigma-Aldrich

二苯甲醇

99%

别名:

α-苯基苯甲醇, 二苯基甲醇, 苯甲醇

登录查看公司和协议定价


About This Item

线性分子式:
(C6H5)2CHOH
CAS号:
分子量:
184.23
Beilstein:
1424379
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

99%

表单

powder

沸点

297-298 °C (lit.)

mp

65-67 °C (lit.)

SMILES字符串

OC(c1ccccc1)c2ccccc2

InChI

1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H

InChI key

QILSFLSDHQAZET-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

应用

二苯基甲醇用于卡宾催化的α,α-二取代羧酸酯的动态动力学拆分。也可用于游离碱和 Ni (II) 卟啉配合物的手性拆分。

储存分类代码

11 - Combustible Solids

WGK

WGK 2

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Carbene-Catalyzed Dynamic Kinetic Resolution of Carboxylic Esters.
Chen X, et al.
Journal of the American Chemical Society, 138(23), 7212-7215 (2016)
Helimeric porphyrinoids: stereostructure and chiral resolution of meso-tetraarylmorpholinochlorins.
Bru?ckner C, et al.
Journal of the American Chemical Society, 133(22), 8740-8752 (2011)
Alkylation of alcohols for gas chromatographic analysis by a phase transfer catalysis technique. Evaluation of benzhydrol benzylation in a one-phase system.
H Brink et al.
Acta pharmaceutica Suecica, 16(4), 247-262 (1979-01-01)
Masanori Ichikawa et al.
Bioorganic & medicinal chemistry, 20(9), 3072-3093 (2012-04-03)
In the present article, we have reported the design, synthesis, and identification of highly potent benzhydrol derivatives as squalene synthase inhibitors (compound 1). Unfortunately, the in vivo efficacies of the compounds were not enough for acquiring the clinical candidate. We
Xiao-Dong Ma et al.
Bioorganic & medicinal chemistry, 19(16), 4704-4709 (2011-07-27)
A series of (±)-benzhydrol derivatives featuring the essential sulfonamide group at the para position on the C-ring were synthesized and evaluated for the potential anti-HIV activity in C8166 cells. Most of these analogues demonstrated low concentration inhibitory activity with EC(50)

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门